Department of Internal Medicine, Baylor Scott & White Medical Center-Temple, 2401 South 31st Street, Temple, TX 76508, USA.
Ohio Northern University Raabe College of Pharmacy, 525 South Main Street, Ada, OH 45810, USA.
Future Oncol. 2020 Oct;16(28):2147-2164. doi: 10.2217/fon-2020-0443. Epub 2020 Jul 21.
The mutation- upregulation- transcription sequence is the principal pathway in the development of renal cell carcinoma. Tyrosine kinase inhibitors target the VEGF receptors to inhibit further growth of renal cell carcinoma tumors. Tivozanib, originally named AV-951 and KRN-951, is a novel, orally bioavailable VEGF tyrosine kinase inhibitor that is selective for VEGF receptors 1, 2 and 3. Further, only picomolar concentrations of tivozanib are required to target these VEGF receptors and prevent phosphorylation; this potency prevents the debilitating side effects that occur with treatments whose mechanisms of action involve broad-spectrum tyrosine kinase inhibition. This review summarizes the growing body of evidence supporting tivozanib's efficacy and safety in the treatment of advanced renal cell carcinoma.
突变-上调-转录序列是肾细胞癌发展的主要途径。酪氨酸激酶抑制剂针对 VEGF 受体,抑制肾细胞癌肿瘤的进一步生长。替沃扎尼布,原名 AV-951 和 KRN-951,是一种新型的、口服生物可利用的 VEGF 酪氨酸激酶抑制剂,对 VEGFR1、2 和 3 具有选择性。此外,仅需皮摩尔浓度的替沃扎尼布即可靶向这些 VEGF 受体并阻止磷酸化;这种效力可防止与作用机制涉及广谱酪氨酸激酶抑制的治疗相关的致残副作用。这篇综述总结了越来越多的证据支持替沃扎尼布在治疗晚期肾细胞癌方面的疗效和安全性。